<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>87</volume><submitter>Huang R</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Metabolic dysfunction is associated with liver disease but it is unclear if it would impact responses to antiviral treatment in chronic hepatitis B (CHB) patients.&lt;h4>Methods&lt;/h4>Using data from an international consortium of 4507 treatment-naïve CHB patients who initiated nucleos(t)ide analogues (NAs) between January 2004 and August 2024 from 32 centers and propensity-score matching (PSM) to balance the background of patients with and without metabolic disease (diabetes, obesity, dyslipidemia, or hypertension), we compared their biochemical (BR), virologic (VR), and complete (CR) response.&lt;h4>Findings&lt;/h4>More than half (54.8%) had at least one metabolic disease. Patients with metabolic disease (vs. no) were older and more likely male. In the PSM cohort of 893 pairs of </pubmed_abstract><journal>EClinicalMedicine</journal><pagination>103407</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12359161</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Impact of metabolic dysfunction on treatment responses to nucleos(t)ide analogues in chronic hepatitis B: a retrospective multi-center REAL-B cohort study.</pubmed_title><pmcid>PMC12359161</pmcid><pubmed_authors>Ito T</pubmed_authors><pubmed_authors>Huang CF</pubmed_authors><pubmed_authors>Wu C</pubmed_authors><pubmed_authors>Enomoto M</pubmed_authors><pubmed_authors>Tsuji K</pubmed_authors><pubmed_authors>Jung JH</pubmed_authors><pubmed_authors>Chuma M</pubmed_authors><pubmed_authors>Huang R</pubmed_authors><pubmed_authors>Kim SE</pubmed_authors><pubmed_authors>Yu ML</pubmed_authors><pubmed_authors>Jun DW</pubmed_authors><pubmed_authors>Yasuda S</pubmed_authors><pubmed_authors>Yeh ML</pubmed_authors><pubmed_authors>Kim GA</pubmed_authors><pubmed_authors>Maeda M</pubmed_authors><pubmed_authors>Tseng CH</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Jeong SW</pubmed_authors><pubmed_authors>Hsu YC</pubmed_authors><pubmed_authors>Takaguchi K</pubmed_authors><pubmed_authors>Inoue K</pubmed_authors><pubmed_authors>Toyoda H</pubmed_authors><pubmed_authors>Itobayashi E</pubmed_authors><pubmed_authors>Abe H</pubmed_authors><pubmed_authors>Atsukawa M</pubmed_authors><pubmed_authors>Chuang WL</pubmed_authors><pubmed_authors>Dai CY</pubmed_authors><pubmed_authors>Nguyen MH</pubmed_authors><pubmed_authors>Oh H</pubmed_authors><pubmed_authors>Liu JK</pubmed_authors><pubmed_authors>Uojima H</pubmed_authors><pubmed_authors>Gadano A</pubmed_authors><pubmed_authors>Senoh T</pubmed_authors><pubmed_authors>Ishigami M</pubmed_authors><pubmed_authors>Huang DQ</pubmed_authors><pubmed_authors>Tanaka Y</pubmed_authors><pubmed_authors>Cheung R</pubmed_authors><pubmed_authors>Yoon E</pubmed_authors><pubmed_authors>Itokawa N</pubmed_authors><pubmed_authors>Kozuka R</pubmed_authors><pubmed_authors>Takahashi H</pubmed_authors><pubmed_authors>Ahn SB</pubmed_authors><pubmed_authors>Nozaki A</pubmed_authors><pubmed_authors>Trinh H</pubmed_authors><pubmed_authors>Ishikawa T</pubmed_authors><pubmed_authors>Watanabe T</pubmed_authors><pubmed_authors>Tsai PC</pubmed_authors><pubmed_authors>Chau A</pubmed_authors><pubmed_authors>Kawashima K</pubmed_authors><pubmed_authors>Vutien P</pubmed_authors><pubmed_authors>Hsiao T</pubmed_authors><pubmed_authors>Marciano S</pubmed_authors><pubmed_authors>Huang JF</pubmed_authors><pubmed_authors>Honda T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Impact of metabolic dysfunction on treatment responses to nucleos(t)ide analogues in chronic hepatitis B: a retrospective multi-center REAL-B cohort study.</name><description>&lt;h4>Background&lt;/h4>Metabolic dysfunction is associated with liver disease but it is unclear if it would impact responses to antiviral treatment in chronic hepatitis B (CHB) patients.&lt;h4>Methods&lt;/h4>Using data from an international consortium of 4507 treatment-naïve CHB patients who initiated nucleos(t)ide analogues (NAs) between January 2004 and August 2024 from 32 centers and propensity-score matching (PSM) to balance the background of patients with and without metabolic disease (diabetes, obesity, dyslipidemia, or hypertension), we compared their biochemical (BR), virologic (VR), and complete (CR) response.&lt;h4>Findings&lt;/h4>More than half (54.8%) had at least one metabolic disease. Patients with metabolic disease (vs. no) were older and more likely male. In the PSM cohort of 893 pairs of </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-05-02T03:49:49.997Z</modification><creation>2026-04-07T17:36:14.834Z</creation></dates><accession>S-EPMC12359161</accession><cross_references><pubmed>40831465</pubmed><doi>10.1016/j.eclinm.2025.103407</doi></cross_references></HashMap>